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Imerslund-Gräsbeck Syndrome: report of two cases in a family
Journal of Clinical Excellence. 2013; 1 (2): 115-122
en Persa | IMEMR | ID: emr-177946
ABSTRACT
Imerslund-Gräsbeck Syndrome is an inherited disorder which present as a megaloblastic anemia followed by selective vitamine B12 deficiency and is associated with mild proteineuria. This rare disease is easily treatable if detected. In this paper two members of a family with Imerslund-Gräsbeck Syndrome are reported
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Índice: IMEMR (Mediterraneo Oriental) Idioma: Persa Revista: J. Clin. Excell. Año: 2013

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Índice: IMEMR (Mediterraneo Oriental) Idioma: Persa Revista: J. Clin. Excell. Año: 2013